Identification and purification of cytolytic antibodies directed against O-acetylated sialic acid in childhood acute lymphoblastic leukemia

被引:45
作者
Pal, S
Chatterjee, M
Bhattacharya, DK
Bandhyopadhyay, S
Mandal, C
机构
[1] Indian Inst Chem Biol, Div Immunobiol, Calcutta 700032, W Bengal, India
[2] Indian Inst Chem Biol, Cellular Immunol Div, Calcutta 700032, W Bengal, India
[3] Vivekananda Inst Med Sci, Calcutta 700045, W Bengal, India
关键词
antibodies against O-acetylated sialic acids; acute lymphoblastic leukemia; bovine submaxillary mucin; cytolysis; 9-O-acetylated sialic acids;
D O I
10.1093/glycob/10.6.539
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Sialic acids typically present as terminal sugars of oligosaccharides are reported to be modified by O-acetylation at the C-9 position on lymphoblasts of childhood acute lymphoblastic leukemia (ALL) patients (Sinha et al,, 1999a, Leukaemia, 13, 11.9-125). We now report high titers of IgG antibodies directed against O-acetylated derivatives of sialic acids (O-AcSA) in serum of ALL patients. These antibodies were purified using bovine submaxillary mucin (BSM) and the IgG distribution was confined to IgC(1) and IgG(2) subclasses; their binding was totally abolished with de-O-acetylation confirming their specificity towards O-AcSA determinants. Flow cytometry demonstrated binding of these antibody fractions to peripheral blood mononuclear cells (PBMC) of both T- and B-ALL patients having increased cell surface 9-O-AcSA determinants. Western blotting of membranes derived from PBMC of ALL patients confirmed binding of the antibody to O-acetylated sialoglycoconjugates corresponding to 144, 135, 126, 90, and 36 kDa whereas binding to PBMC from normal individuals corresponded to 144 and 36 kDa, Specificity of the antibody fraction towards 9-O-AcSA was substantiated by hemagglutination and hemagglutination-inhibition assays. The antibody purified from ALL serum selectively mediates complement dependent cytolysis of lymphoblasts expressing O-AcSAs and thereby possibly confers passive protection. The enhanced anti O-AcSA antibody levels allowed for development of a serodiagnostic assay (BSM-ELISA) specific for ALL. Minimal crossreactivity was observed with other hematological disorders like acute myeloid leukemia (n = 16), chronic myeloid leukemia (n = 6), chronic lymphocytic leukemia (n = 7) and non-Hodgkin's lymphoma (n = 3) as well as normal healthy individuals (n = 28). The BSM-ELISA therefore provides a simple, noninvasive alternative diagnostic approach for ALL and merits clinical consideration.
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收藏
页码:539 / 549
页数:11
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